FDA regulations and the ICH GCP recommendations

Date : 6th March 2018 to 6th March 2018

Place : United States, Fremont

Website :http://www.compliance4all.com/control/w_product/~product_id=501594LIVE?channel=allconferencealerts_Mar_2018_SEO

Contact Person:Event Manager

Description:

Overview: It will be important to see what the FDA regulations and the ICH GCP recommendations are in this regard. The key is that the PI and all clinical staff know and follow the research plan (Protocol) exactly as it is written. To do this is ethical research. To not follow the protocol and document study conduct carelessly is folly. Why should you Attend: All CRO's, Sites, and Sponsors of Clinical Research involved in the drug and device development process have an interest in being prepared for the audit process. Attending this Webinar is a good step toward learning the FDA processes and why the Sponsor's / CRO's Monitors are so important.

FDA regulations and the ICH GCP recommendations will be held in Fremont,United States on date 2018-03-06

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Deadline for abstracts/proposals : 5th March 2018

Keynote Speakers :

Venue :Fremont, CA, United States

Check the event website for more details.